Finne P, Zhang W M, Auvinen A, Leinonen J, Määttänen L, Rannikko S, Tammela T L, Stenman U H
Department of Clinical Chemistry, Helsinki University Central Hospital, Finland.
J Urol. 2000 Dec;164(6):1956-60.
We assess whether the complex between prostate specific antigen (PSA) and alpha1-protease inhibitor in serum can be used to reduce further the number of false-positive PSA screen results independent of total and free PSA.
Sera from 304 consecutive screen positive subjects, including 78 with and 226 without prostate cancer, and serum PSA of 4 to 10 microg./l. or higher in the Finnish, randomized, population based prostate cancer screening trial were analyzed for PSA-alpha-protease inhibitor, and total and free PSA. Main outcome measures were specificity, sensitivity and area under receiver operating characteristics curve for proportions of free PSA and PSA-alpha 1-protease inhibitor, and for a combination of these among screen positive cases.
The proportion of serum PSA-alpha 1-protease inhibitor of total PSA was lower in cancer cases than in controls (0.9% versus 1.6%, p <0.001). Logistic regression analysis of total PSA, free PSA and PSA-alpha 1-protease inhibitor showed that PSA-alpha 1-protease inhibitor in serum was an independent variable for discrimination between subjects with and without prostate cancer (p = 0.006) in the PSA range of 4 to 10 microg./l. The proportion of PSA-alpha 1-protease inhibitor alone improved specificity less than the proportion of free PSA but when these were combined by logistic regression they performed better than the proportion of free PSA alone at sensitivities of 85% to 95% (p <0.001).
Serum PSA-alpha 1-protease inhibitor improves the specificity of total and free PSA in a screening population with total PSA 4 to 10 microg./l.
我们评估血清中前列腺特异性抗原(PSA)与α1-蛋白酶抑制剂的复合物是否可用于进一步减少PSA筛查结果假阳性的数量,且不受总PSA和游离PSA的影响。
在芬兰基于人群的随机前列腺癌筛查试验中,对304例连续筛查阳性受试者的血清进行分析,其中包括78例患有前列腺癌和226例未患前列腺癌的受试者,血清PSA为4至10微克/升或更高,检测PSA-α1-蛋白酶抑制剂、总PSA和游离PSA。主要观察指标为游离PSA和PSA-α1-蛋白酶抑制剂比例的特异性、敏感性和受试者操作特征曲线下面积,以及筛查阳性病例中两者的组合。
癌症患者血清PSA-α1-蛋白酶抑制剂占总PSA的比例低于对照组(0.9%对1.6%,p<0.001)。对总PSA、游离PSA和PSA-α1-蛋白酶抑制剂进行逻辑回归分析显示,在4至10微克/升的PSA范围内,血清中的PSA-α1-蛋白酶抑制剂是区分有无前列腺癌受试者的独立变量(p = 0.006)。单独的PSA-α1-蛋白酶抑制剂比例提高特异性的程度小于游离PSA比例,但通过逻辑回归将两者结合时,在85%至95%的敏感性下,其表现优于单独的游离PSA比例(p<0.001)。
血清PSA-α1-蛋白酶抑制剂可提高总PSA为4至10微克/升的筛查人群中总PSA和游离PSA的特异性。